Home NDC 55154-7702 COUMADIN
Product NDC 55154-7702
11-digit product format 551547702
Labeler code 55154
Product ID 55154-7702_a8ffee52-e235-4af4-a25a-d4dc30b57f3c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name warfarin sodium
Dosage form TABLET
Route ORAL
Labeler Cardinal Health
Application NDA009218
Marketing category NDA
Marketing start 2009-01-01
Marketing end 0000-00-00
Substance WARFARIN SODIUM
Active strength 2 mg/1
Pharmacologic classes Vitamin K Antagonist [EPC],Vitamin K Inhibitors [MoA]
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55154-7702-0 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 55154-7702-0 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 55154-7702-0 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 55154-7702-0 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 55154-7702-0 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 55154-7702-0 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 55154-7702-0 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 55154-7702-0 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 55154-7702-0 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 55154-7702-0 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 55154-7702-0 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 55154-7702-0 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 12 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N009218-005 COUMADIN WARFARIN SODIUM 10MG TABLET / ORAL RLD, Approved before 1982 N009218-007 COUMADIN WARFARIN SODIUM 5MG TABLET / ORAL RLD, Approved before 1982 N009218-012 COUMADIN WARFARIN SODIUM 75MG/VIAL INJECTABLE / INJECTION Approved before 1982 N009218-013 COUMADIN WARFARIN SODIUM 2MG TABLET / ORAL RLD, Approved before 1982 N009218-016 COUMADIN WARFARIN SODIUM 7.5MG TABLET / ORAL RLD, Approved before 1982 N009218-018 COUMADIN WARFARIN SODIUM 2.5MG TABLET / ORAL RLD, Approved before 1982 N009218-020 COUMADIN WARFARIN SODIUM 50MG/VIAL INJECTABLE / INJECTION Approved before 1982 N009218-022 COUMADIN WARFARIN SODIUM 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET / ORAL RLD 1990-03-01 N009218-023 COUMADIN WARFARIN SODIUM 4MG TABLET / ORAL RLD 1993-08-24 N009218-024 COUMADIN WARFARIN SODIUM 5MG/VIAL INJECTABLE / INJECTION 1995-02-07 N009218-025 COUMADIN WARFARIN SODIUM 3MG TABLET / ORAL RLD 1996-11-18 N009218-026 COUMADIN WARFARIN SODIUM 6MG TABLET / ORAL RLD 1996-11-18
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 13 · 504 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-18 06:07:40 2026-07 N009218-005 COUMADIN 10MG TABLET / ORAL RLD, Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-007 COUMADIN 5MG TABLET / ORAL RLD, Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-012 COUMADIN 75MG/VIAL INJECTABLE / INJECTION Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-013 COUMADIN 2MG TABLET / ORAL RLD, Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-016 COUMADIN 7.5MG TABLET / ORAL RLD, Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-018 COUMADIN 2.5MG TABLET / ORAL RLD, Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-020 COUMADIN 50MG/VIAL INJECTABLE / INJECTION Approved before 1982 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-022 COUMADIN 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET / ORAL RLD 1990-03-01 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-023 COUMADIN 4MG TABLET / ORAL RLD 1993-08-24 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-024 COUMADIN 5MG/VIAL INJECTABLE / INJECTION 1995-02-07 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-025 COUMADIN 3MG TABLET / ORAL RLD 1996-11-18 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N009218-026 COUMADIN 6MG TABLET / ORAL RLD 1996-11-18 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N009218-005 COUMADIN 10MG TABLET / ORAL RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-007 COUMADIN 5MG TABLET / ORAL RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-012 COUMADIN 75MG/VIAL INJECTABLE / INJECTION Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-013 COUMADIN 2MG TABLET / ORAL RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-016 COUMADIN 7.5MG TABLET / ORAL RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-018 COUMADIN 2.5MG TABLET / ORAL RLD, Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-020 COUMADIN 50MG/VIAL INJECTABLE / INJECTION Approved before 1982 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-022 COUMADIN 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET / ORAL RLD 1990-03-01 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-023 COUMADIN 4MG TABLET / ORAL RLD 1993-08-24 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-024 COUMADIN 5MG/VIAL INJECTABLE / INJECTION 1995-02-07 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-025 COUMADIN 3MG TABLET / ORAL RLD 1996-11-18 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N009218-026 COUMADIN 6MG TABLET / ORAL RLD 1996-11-18 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-005 COUMADIN 10MG TABLET / ORAL RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-007 COUMADIN 5MG TABLET / ORAL RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-012 COUMADIN 75MG/VIAL INJECTABLE / INJECTION Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-013 COUMADIN 2MG TABLET / ORAL RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-016 COUMADIN 7.5MG TABLET / ORAL RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-018 COUMADIN 2.5MG TABLET / ORAL RLD, Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-020 COUMADIN 50MG/VIAL INJECTABLE / INJECTION Approved before 1982 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-022 COUMADIN 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** TABLET / ORAL RLD 1990-03-01 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-023 COUMADIN 4MG TABLET / ORAL RLD 1993-08-24 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-024 COUMADIN 5MG/VIAL INJECTABLE / INJECTION 1995-02-07 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-025 COUMADIN 3MG TABLET / ORAL RLD 1996-11-18 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N009218-026 COUMADIN 6MG TABLET / ORAL RLD 1996-11-18 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N009218-005 COUMADIN 10MG TABLET / ORAL RLD, Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N009218-007 COUMADIN 5MG TABLET / ORAL RLD, Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N009218-012 COUMADIN 75MG/VIAL INJECTABLE / INJECTION Approved before 1982 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N009218-013 COUMADIN 2MG TABLET / ORAL RLD, Approved before 1982 6a471c1ec25d…
Observed Orange Book normalized TE history# DailyMed Socrata Ingredients# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55154-7702-0 55154770200 10 BLISTER PACK in 1 BAG (55154-7702-0) > 1 TABLET in 1 BLISTER PACK 10 blister pack 2009-01-01 0000-00-00 No No Current